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40106-12-5

40106-12-5 Structure

40106-12-5 Structure
IdentificationBack Directory
[Name]

2-AMINO-5,6,7,8-TETRAHYDRO-4H-CYCLOHEPTA[B]THIOPHENE-3-CARBOXAMIDE
[CAS]

40106-12-5
[Synonyms]

NSC727447
2-Amino-4H,5H,6H,7H,8H-cyclohepta[b]thiophene-3-carboxamide
2-amino-5,6,7,8-tetrahydro-4H-cyclohepta[d]thiophene-3-carboxamide
[Molecular Formula]

C10H14N2OS
[MDL Number]

MFCD00622214
[MOL File]

40106-12-5.mol
[Molecular Weight]

210.3
Chemical PropertiesBack Directory
[Melting point ]

154-156 °C(Solv: ethanol (64-17-5))
[Boiling point ]

347.5±42.0 °C(Predicted)
[density ]

1.278±0.06 g/cm3(Predicted)
[storage temp. ]

room temp
[solubility ]

DMSO: >10mg/mL
[form ]

Solid
[pka]

15.70±0.20(Predicted)
[color ]

Light brown to brown
[InChI]

1S/C10H14N2OS/c11-9(13)8-6-4-2-1-3-5-7(6)14-10(8)12/h1-5,12H2,(H2,11,13)
[InChIKey]

LULYZYNTDPUEKK-UHFFFAOYSA-N
[SMILES]

NC(=O)c1c(N)sc2CCCCCc12
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Hazard InformationBack Directory
[Uses]

NSC727447 is an inhibitor of ribonuclease H (Rnase H) of HIV-1 and HIV-2. NSC727447 has little activity against E. coli RNase H, but great selectivity over human Rnase H, with IC50s value of 2.0 μM, 2.5 μM, 100 μM, 10.6 μM, respectively[1].
[Biological Activity]

NSC727447 is an inhibitor of ribonuclease H (Rnase H) of HIV-1 and HIV-2. NSC727447 has little activity against E. coli RNase Hbut gre at selectivity over human Rnase H.
[References]

[1] Michaela Wendeler, et al. Vinylogous Ureas as a Novel Class of Inhibitors of Reverse Transcriptase-Associated Ribonuclease H Activity. ACS Chem Biol. 2008 Oct 17;3(10):635-44. DOI:10.1021/cb8001039
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